NP-MRD: Showing NP-Card for 5-Amino-6-(5-phosphoribosylamino)uracil (NP0062934)

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Record Information

Version

2.0

Created at

2022-04-28 07:27:23 UTC

Updated at

2022-04-28 07:27:23 UTC

NP-MRD ID

NP0062934

Secondary Accession Numbers

None

Natural Product Identification

Common Name

5-Amino-6-(5-phosphoribosylamino)uracil

Description

{[(2S,3S,4R,5R)-5-[(5-amino-2,6-dihydroxypyrimidin-4-yl)amino]-3,4-dihydroxyoxolan-2-yl]methoxy}phosphonic acid belongs to the class of organic compounds known as pentose phosphates. These are carbohydrate derivatives containing a pentose substituted by one or more phosphate groups. 5-Amino-6-(5-phosphoribosylamino)uracil is found in Escherichia coli. Based on a literature review very few articles have been published on {[(2S,3S,4R,5R)-5-[(5-amino-2,6-dihydroxypyrimidin-4-yl)amino]-3,4-dihydroxyoxolan-2-yl]methoxy}phosphonic acid.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 38 39  0  0  0  0  0  0  0  0999 V2000
   -4.6454   -0.6129   -1.4659 N   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0857    0.0234   -0.3241 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7169    0.1188   -0.1523 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8586   -0.4451   -1.1469 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4275   -0.4174   -1.1207 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.1490   -0.9396   -0.0007 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.2629   -0.2542    0.3148 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.4890   -1.1435    0.5016 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5444   -0.3066    0.8186 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.9915   -1.1112    1.0630 P   0  0  2  0  0  5  0  0  0  0  0  0
    5.0176   -2.4116    0.2852 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.1051   -1.4484    2.7360 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.3361   -0.1834    0.6630 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5781    0.6706   -0.8118 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.3584    0.0286   -1.7578 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1704    0.9480   -1.3619 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.3287    1.2278   -2.7063 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2573    0.7321    0.9486 N   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0604    1.2654    1.9048 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5681    1.8366    2.9299 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3845    1.1573    1.7102 N   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9081    0.5581    0.6349 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1596    0.4702    0.4767 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8514   -1.6157   -1.4549 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8518   -0.0657   -2.3256 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3509   -0.9150   -1.9591 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1075   -1.0522   -2.0162 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0884    0.3072    1.2748 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6975   -1.7072   -0.4044 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.3270   -1.8435    1.3329 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2521   -0.5488    3.1638 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1540    0.7743    0.8905 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0190    1.6349   -0.4899 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9138   -0.7957   -2.0519 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2645    1.7587   -0.7941 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9987    1.9177   -2.8689 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2454    0.8262    1.1286 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0384    1.5618    2.4355 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  6  7  1  0
  7  8  1  0
  8  9  1  0
 10  9  1  1
 10 12  1  0
 10 13  1  0
 10 11  2  0
  7 14  1  0
 14 15  1  0
 14 16  1  0
 16 17  1  0
  3 18  1  0
 18 19  1  0
 19 20  2  0
 19 21  1  0
 21 22  1  0
 22 23  2  0
 22  2  1  0
 16  5  1  0
  1 24  1  0
  1 25  1  0
  4 26  1  0
  5 27  1  6
  7 28  1  1
  8 29  1  0
  8 30  1  0
 12 31  1  0
 13 32  1  0
 14 33  1  1
 15 34  1  0
 16 35  1  1
 17 36  1  0
 18 37  1  0
 21 38  1  0
M  END


  Mrv1652304282209272D          

 23 24  0  0  1  0            999 V2000
   -0.6078   -1.2991    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.0597   -1.7840    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.1953   -2.5687    0.0000 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.0203   -2.5687    0.0000 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.2752   -1.7840    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5052   -3.2361    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1696   -3.9898    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3491   -4.0760    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0136   -4.8297    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8069   -4.9159    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4985   -5.4971    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3190   -5.4109    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8039   -6.0783    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6546   -4.6572    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4750   -4.5710    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    0.2897   -3.2361    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8443   -1.5291    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6078   -0.4741    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1067   -0.0616    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1067    0.7634    0.0000 P   0  0  0  0  0  0  0  0  0  0  0  0
    0.1067    1.5884    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.9317    0.7634    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7183    0.7634    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  3  4  1  0  0  0  0
  4  5  1  0  0  0  0
  1  5  1  0  0  0  0
  4  6  1  6  0  0  0
  6  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  2  0  0  0  0
  9 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 12 14  1  0  0  0  0
  7 14  2  0  0  0  0
 14 15  1  0  0  0  0
  3 16  1  1  0  0  0
  2 17  1  1  0  0  0
  1 18  1  1  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  2  0  0  0  0
 20 22  1  0  0  0  0
 20 23  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0062934

> <DATABASE_NAME>
NP-MRD

> <SMILES>
NC1=C(N[C@@H]2O[C@@H](COP(O)(O)=O)[C@@H](O)[C@H]2O)NC(=O)NC1=O

> <INCHI_IDENTIFIER>
InChI=1S/C9H15N4O9P/c10-3-6(12-9(17)13-7(3)16)11-8-5(15)4(14)2(22-8)1-21-23(18,19)20/h2,4-5,8,14-15H,1,10H2,(H2,18,19,20)(H3,11,12,13,16,17)/t2-,4+,5+,8+/m0/s1

> <INCHI_KEY>
LZEXYCAGPMYXLX-MSTUQOROSA-N

> <FORMULA>
C9H15N4O9P

> <MOLECULAR_WEIGHT>
354.212

> <EXACT_MASS>
354.057665077

> <JCHEM_ACCEPTOR_COUNT>
10

> <JCHEM_ATOM_COUNT>
38

> <JCHEM_AVERAGE_POLARIZABILITY>
29.530018039083416

> <JCHEM_BIOAVAILABILITY>
0

> <JCHEM_DONOR_COUNT>
8

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
{[(2S,3S,4R,5R)-5-[(5-amino-2,6-dioxo-1,2,3,6-tetrahydropyrimidin-4-yl)amino]-3,4-dihydroxyoxolan-2-yl]methoxy}phosphonic acid

> <ALOGPS_LOGP>
-1.84

> <JCHEM_LOGP>
-3.7151084476666667

> <ALOGPS_LOGS>
-1.99

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-2

> <JCHEM_PKA>
6.248803119147886

> <JCHEM_PKA_STRONGEST_ACIDIC>
1.2255771173733017

> <JCHEM_PKA_STRONGEST_BASIC>
-3.6640269455988914

> <JCHEM_POLAR_SURFACE_AREA>
212.69999999999996

> <JCHEM_REFRACTIVITY>
79.87729999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
3.64e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
[(2S,3S,4R,5R)-5-[(5-amino-2,6-dioxo-1,3-dihydropyrimidin-4-yl)amino]-3,4-dihydroxyoxolan-2-yl]methoxyphosphonic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 28-APR-22   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   28-APR-22         0                                  
HETATM    1  C   UNK     0      -1.134  -2.425   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       0.111  -3.330   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -0.364  -4.795   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -1.904  -4.795   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0      -2.380  -3.330   0.000  0.00  0.00           O+0
HETATM    6  N   UNK     0      -2.810  -6.041   0.000  0.00  0.00           N+0
HETATM    7  C   UNK     0      -2.183  -7.448   0.000  0.00  0.00           C+0
HETATM    8  N   UNK     0      -0.652  -7.609   0.000  0.00  0.00           N+0
HETATM    9  C   UNK     0      -0.025  -9.015   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       1.506  -9.176   0.000  0.00  0.00           O+0
HETATM   11  N   UNK     0      -0.931 -10.261   0.000  0.00  0.00           N+0
HETATM   12  C   UNK     0      -2.462 -10.100   0.000  0.00  0.00           C+0
HETATM   13  O   UNK     0      -3.367 -11.346   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0      -3.088  -8.693   0.000  0.00  0.00           C+0
HETATM   15  N   UNK     0      -4.620  -8.532   0.000  0.00  0.00           N+0
HETATM   16  O   UNK     0       0.541  -6.041   0.000  0.00  0.00           O+0
HETATM   17  O   UNK     0       1.576  -2.854   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0      -1.134  -0.885   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       0.199  -0.115   0.000  0.00  0.00           O+0
HETATM   20  P   UNK     0       0.199   1.425   0.000  0.00  0.00           P+0
HETATM   21  O   UNK     0       0.199   2.965   0.000  0.00  0.00           O+0
HETATM   22  O   UNK     0       1.739   1.425   0.000  0.00  0.00           O+0
HETATM   23  O   UNK     0      -1.341   1.425   0.000  0.00  0.00           O+0
CONECT    1    2    5   18                                                  
CONECT    2    1    3   17                                                  
CONECT    3    2    4   16                                                  
CONECT    4    3    5    6                                                  
CONECT    5    4    1                                                       
CONECT    6    4    7                                                       
CONECT    7    6    8   14                                                  
CONECT    8    7    9                                                       
CONECT    9    8   10   11                                                  
CONECT   10    9                                                            
CONECT   11    9   12                                                       
CONECT   12   11   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12    7   15                                                  
CONECT   15   14                                                            
CONECT   16    3                                                            
CONECT   17    2                                                            
CONECT   18    1   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21   22   23                                             
CONECT   21   20                                                            
CONECT   22   20                                                            
CONECT   23   20                                                            
MASTER        0    0    0    0    0    0    0    0   23    0   48    0
END

View in JSmol

Synonyms

Value	Source
{[(2S,3S,4R,5R)-5-[(5-amino-2,6-dihydroxypyrimidin-4-yl)amino]-3,4-dihydroxyoxolan-2-yl]methoxy}phosphonate	Generator

Chemical Formula

C₉H₁₅N₄O₉P

Average Mass

354.2120 Da

Monoisotopic Mass

354.05767 Da

IUPAC Name

{[(2S,3S,4R,5R)-5-[(5-amino-2,6-dioxo-1,2,3,6-tetrahydropyrimidin-4-yl)amino]-3,4-dihydroxyoxolan-2-yl]methoxy}phosphonic acid

Traditional Name

[(2S,3S,4R,5R)-5-[(5-amino-2,6-dioxo-1,3-dihydropyrimidin-4-yl)amino]-3,4-dihydroxyoxolan-2-yl]methoxyphosphonic acid

CAS Registry Number

Not Available

SMILES

NC1=C(N[C@@H]2O[C@@H](COP(O)(O)=O)[C@@H](O)[C@H]2O)NC(=O)NC1=O

InChI Identifier

InChI=1S/C9H15N4O9P/c10-3-6(12-9(17)13-7(3)16)11-8-5(15)4(14)2(22-8)1-21-23(18,19)20/h2,4-5,8,14-15H,1,10H2,(H2,18,19,20)(H3,11,12,13,16,17)/t2-,4+,5+,8+/m0/s1

InChI Key

LZEXYCAGPMYXLX-MSTUQOROSA-N

Experimental Spectra

Not Available

Predicted Spectra

Spectrum Type	Description	Depositor ID	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 25 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Escherichia coli	Bacteria	KNApSAcK

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as pentose phosphates. These are carbohydrate derivatives containing a pentose substituted by one or more phosphate groups.

Kingdom

Organic compounds

Super Class

Organic oxygen compounds

Class

Organooxygen compounds

Sub Class

Carbohydrates and carbohydrate conjugates

Direct Parent

Pentose phosphates

Alternative Parents

Substituents

Pentose-5-phosphate
Pentose phosphate
N-glycosyl compound
Glycosyl compound
Monosaccharide phosphate
Hydroxypyrimidine
Monoalkyl phosphate
Secondary aliphatic/aromatic amine
Aminopyrimidine
Imidolactam
Alkyl phosphate
Pyrimidine
Phosphoric acid ester
Organic phosphoric acid derivative
Heteroaromatic compound
Tetrahydrofuran
Secondary alcohol
1,2-diol
Oxacycle
Azacycle
Organoheterocyclic compound
Secondary amine
Organic nitrogen compound
Organopnictogen compound
Organic oxide
Hydrocarbon derivative
Primary amine
Organonitrogen compound
Amine
Alcohol
Aromatic heteromonocyclic compound

Molecular Framework

Aromatic heteromonocyclic compounds

External Descriptors

Not Available

Physical Properties

State

Not Available

Experimental Properties

Property	Value	Reference
Melting Point	Not Available	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	Not Available	Not Available
LogP	Not Available	Not Available

Predicted Properties

Property	Value	Source
logP	-1.8	ALOGPS
logP	-3.7	ChemAxon
logS	-2	ALOGPS
pKa (Strongest Acidic)	1.23	ChemAxon
pKa (Strongest Basic)	-3.7	ChemAxon
Physiological Charge	-2	ChemAxon
Hydrogen Acceptor Count	10	ChemAxon
Hydrogen Donor Count	8	ChemAxon
Polar Surface Area	212.7 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	79.88 m³·mol⁻¹	ChemAxon
Polarizability	29.53 Å³	ChemAxon
Number of Rings	2	ChemAxon
Bioavailability	No	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

162822835

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Not Available

Showing NP-Card for 5-Amino-6-(5-phosphoribosylamino)uracil (NP0062934)

MOL for NP0062934 (5-Amino-6-(5-phosphoribosylamino)uracil)

3D MOL for NP0062934 (5-Amino-6-(5-phosphoribosylamino)uracil)

3D SDF for NP0062934 (5-Amino-6-(5-phosphoribosylamino)uracil)

3D-SDF for NP0062934 (5-Amino-6-(5-phosphoribosylamino)uracil)

PDB for NP0062934 (5-Amino-6-(5-phosphoribosylamino)uracil)

3D PDB for NP0062934 (5-Amino-6-(5-phosphoribosylamino)uracil)

SMILES for NP0062934 (5-Amino-6-(5-phosphoribosylamino)uracil)

INCHI for NP0062934 (5-Amino-6-(5-phosphoribosylamino)uracil)

Structure for NP0062934 (5-Amino-6-(5-phosphoribosylamino)uracil)

3D Structure for NP0062934 (5-Amino-6-(5-phosphoribosylamino)uracil)